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Trial · NCT07889466

Registered outcomes17

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryChange from Baseline and Placebo in Total Sleep Time6 weeks, nightly in baseline, placebo, and intervention.Smartwatch-derived objective total sleep time in minutes.
PrimaryChange from Baseline and Placebo in the Count of Lapse in Psychomotor Vigilance Task (PVT)6 weeks, daily in baseline, placebo, and intervention.Count of responses with reaction time greater than 500 milliseconds in a PVT session.
PrimaryChange from Baseline and Placebo in Subjective Sleep Quality6 weeks, daily in baseline, placebo, and intervention.Self-reported sleep quality score on a visual analogue scale of 0 to 100, higher indicating more favorable.
SecondaryChange from Baseline and Placebo in Sleep Efficiency6 weeks, nightly in baseline, placebo, and intervention.Objective total sleep time divided by time in bed, in percentage points.
SecondaryChange from Baseline and Placebo in Sleep Fragmentation Index6 weeks, nightly in baseline, placebo, and intervention.Waking bouts per 100 min of objective total sleep time.
SecondaryChange from Baseline and Placebo in Wake After Sleep Onset6 weeks, nightly in baseline, placebo, and intervention.Objective total time awake after sleep onset and before wake onset, in minutes.
SecondaryChange from Baseline and Placebo in Deep Sleep Duration6 weeks, nightly in baseline, placebo, and intervention.Smartwatch-derived deep sleep duration in minutes.
SecondaryChange from Baseline and Placebo in Deep Sleep Percentage6 weeks, nightly in baseline, placebo, and intervention.Smartwatch-derived deep sleep in percentage of objective total sleep time.
SecondaryChange from Baseline and Placebo in Rapid Eye Movement (REM) Sleep Duration6 weeks, nightly in baseline, placebo, and intervention.Smartwatch-derived REM sleep duration in minutes.
SecondaryChange from Baseline and Placebo in Rapid Eye Movement (REM) Sleep Percentage6 weeks, nightly in baseline, placebo, and intervention.Smartwatch-derived REM sleep in percentage of objective total sleep time.
SecondaryChange from Baseline and Placebo in Mean Response Speed6 weeks, daily in baseline, placebo, and intervention.Mean reciprocal reaction time in a PVT session, in per second.
SecondaryChange from Baseline and Placebo in Mean Slowest-10% Response Speed6 week, daily in baseline, placebo, and intervention.Mean reciprocal reaction time over the slowest 10% responses in a PVT session, in per second.
SecondaryChange from Baseline and Placebo in Subjective Alertness6 weeks, daily in baseline, placebo, and intervention.Daily self-reported alertness score on a visual analogue scale of 0 to 100, higher indicating more favorable.
SecondaryChange from Baseline and Placebo in Subjective Happiness6 weeks, daily in baseline, placebo, and intervention.Self-reported happiness score on a visual analogue scale of 0 to 100, higher indicating more favorable.
SecondaryChange from Baseline and Placebo in Subjective Energy6 weeks, daily in baseline, placebo, and intervention.Self-reported energy score on a visual analogue scale of 0 to 100, higher indicating more favorable.
SecondaryChange from Baseline and Placebo in Subjective Health6 weeks, daily in baseline, placebo, and intervention.Self-reported health score on a visual analogue scale of 0 to 100, higher indicating more favorable.
SecondaryChange from Baseline and Placebo in Subjective Calmness6 weeks, daily in baseline, placebo, and intervention.Self-reported calmness score on a visual analogue scale of 0 to 100, higher indicating more favorable.

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

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Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT07889466/registered